Tert-butyl(4-chloro-2-ethynylphenoxy)acetate → {4-Chloro-2-[(4-hexylpyridin-3-yl)ethynyl]phenoxy}acetic acid
反応式
C([O:5][C:6](=[O:18])[CH2:7][O:8][C:9]1[CH:14]=[CH:13][C:12]([Cl:15])=[CH:11][C:10]=1[C:16]#[CH:17])(C)(C)C.Br[C:20]1[CH:21]=[N:22][CH:23]=[CH:24][C:25]=1[CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH3:31]>>[Cl:15][C:12]1[CH:13]=[CH:14][C:9]([O:8][CH2:7][C:6]([OH:5])=[O:18])=[C:10]([C:16]#[C:17][C:20]2[CH:21]=[N:22][CH:23]=[CH:24][C:25]=2[CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH3:31])[CH:11]=1参加物
3
実験手順
Following the general method as outlined in Example 8, starting from tert-butyl(4-chloro-2-ethynylphenoxy)acetate (Intermediate 3) and 3-bromo-4-hexylpyridine (Intermediate 13), the title compound was obtained as a beige solid after purification by preparative HPLC.
出典と根拠
- ORDレコード
- ord-0896e4b5527b469eb69e4ed1da398c6a
- 出典データセット
- uspto-grants-2012_09